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肿瘤生长和治疗抵抗动力学建模可明确非小细胞肺癌对吉非替尼或化疗的不同反应。

Modeling Tumor Growth and Treatment Resistance Dynamics Characterizes Different Response to Gefitinib or Chemotherapy in Non-Small Cell Lung Cancer.

机构信息

Clinical Pharmacology & Safety Sciences, R&D, AstraZeneca, Boston, Massachusetts, USA.

出版信息

CPT Pharmacometrics Syst Pharmacol. 2020 Mar;9(3):143-152. doi: 10.1002/psp4.12490. Epub 2020 Feb 7.

Abstract

Differences in the effect of gefitinib and chemotherapy on tumor burden in non-small cell lung cancer remain to be fully understood. Using a Bayesian hierarchical model of tumor size dynamics, we estimated the rates of tumor growth and treatment resistance for patients in the Iressa Pan-Asia Study study (NCT00322452). The following relationships characterize greater efficacy of gefitinib in epidermal growth factor receptor (EGFR) positive tumors: Maximum drug effect is, in decreasing order, gefitinib in EGFR-positive, chemotherapy in EGFR-positive, chemotherapy in EGFR-negative, and gefitinib in EGFR-negative tumors; the rate of resistance emergence is, in increasing order: gefitinib in EGFR positive, chemotherapy in EGFR positive, while each is plausibly similar to the rate in EGFR negative tumors, which are estimated with less certainty. The rate of growth is smaller in EGFR-positive than in EGFR-negative fully resistant tumors, regardless of treatment. The model can be used to compare treatment effects and resistance dynamics among different drugs.

摘要

吉非替尼和化疗对非小细胞肺癌肿瘤负荷的影响差异仍有待充分了解。本研究采用肿瘤大小动态的贝叶斯分层模型,对 Iressa Pan-Asia 研究(NCT00322452)中患者的肿瘤生长和治疗耐药率进行了估计。以下关系表明吉非替尼在表皮生长因子受体(EGFR)阳性肿瘤中的疗效更好:最大药物效应依次为 EGFR 阳性的吉非替尼、EGFR 阳性的化疗、EGFR 阴性的化疗和 EGFR 阴性的吉非替尼;耐药出现的速度依次为:EGFR 阳性的吉非替尼、EGFR 阳性的化疗,而每个速度都与 EGFR 阴性肿瘤的速度相似,后者的估计不确定性较大。无论治疗方式如何,EGFR 阳性完全耐药肿瘤的生长速度均小于 EGFR 阴性肿瘤。该模型可用于比较不同药物的治疗效果和耐药动力学。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18f0/7080537/f08dafdd80b4/PSP4-9-143-g001.jpg

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